Canonical Allele Identifier: PA2825640089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2852532
ClinVar RCV Id: RCV003743093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1115Gly
CA16028780
NM_001127511.3:c.3344A>G